Conformable and die-cuttable biaxially oriented films and labelstocks

ABSTRACT

One embodiment of this invention is a die-cuttable, biaxially stretch-oriented monolayer film comprising a polyethylene having a density of about 0.940 g/cm 3  or less, a propylene polymer or copolymer, or mixtures thereof, wherein the tensile modulus of the film in the machine direction is greater than the tensile modulus in the cross direction, the tensile modulus of the film in the cross direction is about 150,000 psi or less, and the film is free of copolymers of ethylene with an ethylenically unsaturated carboxylic acid or ester. In one embodiment, the biaxially oriented monolayer films have been biaxially stretch-oriented and heat set.  
     In another embodiment, the invention relates to a die-cuttable, stretch-oriented multilayer film comprising  
     (A) a base layer having an upper surface and a lower surface, and comprising polyethylene having a density of about 0.940 g/cm 3  or less, a propylene homopolymer or copolymer, or mixtures thereof wherein the base layer is free of copolymers of ethylene with an ethylenically unsaturated carboxylic acid or ester, and  
     (B) a first skin layer of a thermoplastic polymer bonded to the upper surface of the base layer, wherein the tensile modulus of the multilayer film in the machine direction is greater than the tensile modulus in the cross direction, and the tensile modulus in the cross direction is about 150,000 psi or less. The biaxially oriented multilayer films are useful in particular in preparing adhesive containing labelstock for use in adhesive labels.  
     In yet another embodiment, the invention relates to a die-cuttable, biaxially stretch-oriented monolayer film comprising at least one polyolefin wherein the film has been stretch-oriented in the machine direction at a stretch ratio of about 9:1 to about 10:1, and in the cross direction at a stretch ratio of from greater than 1:1 to about 3:1.

FIELD OF THE INVENTION

[0001] This invention relates to conformable and die-cuttable biaxiallyoriented films and labelstocks, and more particularly to biaxiallystretch-oriented monolayer and multilayer films and labelstocks.

BACKGROUND OF THE INVENTION

[0002] It has long been known to manufacture and distributepressure-sensitive adhesive stock for labels by providing a layer offace or facestock material for the label or sign backed by a layer ofpressure-sensitive adhesive which in turn is covered by a release lineror carrier. The liner or carrier protects the adhesive during shipmentand storage and allows for efficient handling of an array of individuallabels after the labels are die-cut and the matrix is stripped from thelayer of facestock material and up to the point where the individuallabels are dispensed in sequence on a labeling line. During the timefrom die-cutting to dispensing, the liner or carrier remains uncut andmay be rolled and unrolled for storage, transit and deployment of thearray of individual labels carried thereon.

[0003] Failure to reliably dispense is typically characterized by thelabel following the carrier around a peel plate without dispensing or“standing-off” from the carrier for application to the substrate. Suchfailure to dispense is believed to be associated with excessive releasevalues between the label facestock material and the liner.Dispensability also is dependent upon the stiffness of the facestock.Failure to dispense may also be characterized by the wrinkling of thelabel due to lack of label stiffness at the dispensing speed as it istransferred from the carrier to the substrate. Another particular needin many labeling applications is the ability to apply polymeric-filmlabels at high line speeds, since an increase in line speed has obviouscost saving advantages.

[0004] In many label applications, it is desirable that the facestockmaterial be a film of polymeric material which can provide propertieslacking in paper, such as clarity, durability, strength,water-resistance, abrasion-resistance, gloss and other properties.Historically, polymeric facestock material of thicknesses greater thanabout 3 mils (75 microns) have been used in order to assuredispensability in automatic labeling apparatuses. For example,plasticized polyvinyl chloride films about 3.5 to 4.0 mils (87.5 to 100microns) thick were used in label application because these filmsexhibited the desired flexibility characteristics. However, themigration of the plasticizers used in PVC films to convert the normallyrigid films to flexible films was recognized as a major problem area forthese types of films resulting in loss of desirable properties such asadhesion, color buildup, shrinkage, and flexibility. Eventually,migration of the plasticizer results in wrinkling, cracking and visualdeterioration of the facestock and/or label. Also, it is desirable toreduce the thickness or “down-gauge” the facestock material in order toattain savings in material costs. Such reduction in facestock thicknessoften has resulted in reduced stiffness and the inability to die-cut anddispense the labels in a reliable commercially acceptable manner usingautomatic machinery. There also was pressure for environmental reasonsto prepare labels from polymer facestocks other than polyvinyl chloride.

[0005] Polymeric materials suggested in the prior art as useful inpreparing labels include biaxially-oriented polypropylene (“BOPP”) ofthicknesses down to about 2.0 mils (50 microns). These materials providecost savings as they are relatively inexpensive, and they havesufficient stiffness to dispense well. However, these materials alsohave relatively high tensile modulus values in both machine-direction(MD) and cross direction (CD) which results in labels which are not veryconformable.

[0006] Related conformability problems have been encountered in respectto rigid surfaces such as glass. For example, when biaxially-orientedfilms are applied to rigid substrates such as glass bottles, theapplication is not completely successful. The relatively stiff labelshave a tendency to bridge surface depressions and the mold seamsresulting from bottle-forming processes resulting in an undesirablesurface appearance of the applied label simulating trapped air bubbles.This has somewhat impeded the use of pressure-sensitive adhesive labelsto replace prior glass bottle labeling techniques such as ceramic inkdirectly bonded to the bottle surface during glass bottle manufacturingprocesses as customers find the appearance unattractive. Such ceramicink techniques are environmentally undesirable due to objectionable inkcomponents and the contamination of the ink in the crushed bottle glassin recycling processes. Attempts to use the relatively stiff orientedpolypropylene films on flexible substrates such as plastic bottles alsohave not been completely successful because the labels do not have theflexibility required to conform to the flexible plastic containers.Oriented polypropylene films are also more difficult to print than PVCor polyethylene films.

[0007] Other useful materials are unoriented polyethylene andpolypropylene films that are also relatively inexpensive andconformable. However, both of these films are difficult to die-cut anddo not dispense well at low calipers. In Europe, an unoriented,relatively thick polyethylene facestock has been used successfully inpreparing labels. The facestock is die-cuttable and the labels can bedispensed in high speed automatic dispensing equipment. The normalthickness of this “standard” polyethylene facestock in Europe is about4.0 mils (100 microns). Attempts to reduce the gauge of the polyethylenefacestock to reduce costs has not yet met with any degree of successbecause the thinner polyethylene facestock is not readily die-cuttablewith the die leaving a mark on the liner and stringers on the cut label.Additionally, the thinner facestock becomes difficult to dispense athigher speeds over a peel plate because of reduced stiffness.

SUMMARY OF THE INVENTION

[0008] One embodiment of this invention is a die-cuttable, biaxiallystretch-oriented monolayer film comprising a polyethylene having adensity of about 0.940 g/cm³ or less, a propylene polymer or copolymer,or mixtures thereof, wherein the tensile modulus of the film in themachine direction is greater than the tensile modulus in the crossdirection, the tensile modulus of the film in the cross direction isabout 150,000 psi or less, and the film is free of copolymers ofethylene with an ethylenically unsaturated carboxylic acid or ester. Inone embodiment, the biaxially oriented monolayer films have beenbiaxially stretch-oriented and heat set.

[0009] In another embodiment, the invention relates to a die-cuttable,stretch-oriented multilayer film comprising

[0010] (A) a base layer having an upper surface and a lower surface, andcomprising polyethylene having a density of about 0.940 g/cm³ or less, apropylene homopolymer or copolymer, or mixtures thereof wherein the baselayer is free of copolymers of ethylene with an ethylenicallyunsaturated carboxylic acid or ester, and

[0011] (B) a first skin layer of a thermoplastic polymer bonded to theupper surface of the base layer, wherein the tensile modulus of themultilayer film in the machine direction is greater than the tensilemodulus in the cross direction, and the tensile modulus in the crossdirection is about 150,000 psi or less. The biaxially orientedmultilayer films are useful in particular in preparing adhesivecontaining labelstock for use in adhesive labels.

[0012] In yet another embodiment, the invention relates to adie-cuttable, biaxially stretch-oriented monolayer film comprising atleast one polyolefin wherein the film has been stretch-oriented in themachine direction at a stretch ratio of about 9:1 to about 10:1, and inthe cross direction at a stretch ratio of from greater than 1:1 to about3:1.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0013] The present invention, in one embodiment, relates to thediscovery that biaxially stretch-oriented monolayer and multilayer filmscan be prepared which are characterized as having improvedconformability, die-cuttability, and/or dispensability. In someembodiments, films having improved clarity can be prepared. Althoughconformable films usually have poor die-cutting properties, the presentinvention provides conformable films that have acceptable die-cuttingproperties, and, therefore, these films may be used for labeling bottlesand tubes or in other label applications that require clarity andconformability. Multilayered film constructions can be prepared inaccordance with the present invention having skin layers designed toprovide printability, or to provide other desirable characteristics suchas stiffness so that the film can be down gauged, or both.

[0014] In one embodiment, the biaxially stretch-oriented monolayer filmsof the present invention comprise a polyethylene having a density ofabout 0.940 g/cm³ or less, a propylene polymer or copolymer, or mixturesthereof, wherein the tensile modulus of the film in the machinedirection is greater than the tensile modulus in the cross direction,the tensile modulus of the film in the cross direction is about 150,000psi or less, and the film is free of copolymers of ethylene with anethylenically unsaturated carboxylic acid or ester.

[0015] Useful ethylene homopolymers include those having densities ofabout 0.940 or less. Polyethylenes having densities of from 0.850 toabout 0.925 g/cm³ generally are referred to as low densitypolyethylenes, and polyethylenes having densities between about 0.925and 0.940 g/cm³ are referred to in the art as being medium densitypolyethylenes. The low and medium density polyethylenes also may becharacterized as having a melt index (as determined by ASTM Test D1238,condition E) in the range of from 0.5 to about 25. In addition to theabove densities, and melt indices, the low density polyethylenes may becharacterized by tensile strengths of between about 2200 to about 3200psi (typically about 2700 psi), and the medium density polyethylenes maybe characterized as having tensile strengths of between about 3000 andabout 4000 psi (typically about 3400 psi).

[0016] Low and medium density polyethylene useful in the first skinlayer of the facestock of this invention are available commercially froma variety of sources. Examples of useful polyethylenes are summarized inthe following Table I. TABLE I Commercial Polyethylenes Commercial MeltIndex Designation Company (g/10 mins) Density (g/cm³) Rexene 1017 Rexene2.0 0.920 Rexene 1058 Rexene 5.5 0.922 Rexene 1080 Rexene 2.0 0.930Rexene 2030 Rexene 5.0 0.919 Rexene 2034 Rexene 7.5 0.925 Rexene 2038Rexene 9.0 0.917 Rexene 2040 Rexene 12.0 0.917 Rexene 2049 Rexene 20.00.917 NA-334 Equistar 6.0 0.918 NA-217 Equistar 5.5 0.923 NA 285-003Equistar 6.2 0.930 Exact 3027 Exxon 3.5 0.900 Exact 3022 Exxon 9.0 0.905Exact 3139 Exxon 7.5 0.900 SLP 9053 Exxon 7.5 0.900 Affinity PF1140 DowChemical 1.6 0.895 Sclair 11G1 Nova 0.72 0.920 Dowlex 2027 Dow Chemical4.0 0.941

[0017] The monolayer film may comprise a propylene homopolymer orcopolymer, or a blend of a propylene homopolymer and at least onepropylene copolymer. When blends of homopolymers and copolymers are usedin the film, the blends may comprise from about 5% to about 95% of thehomopolymer and correspondingly from about 95% to about 5% by weight ofthe copolymer. The propylene homopolymers which may be utilized eitheralone or in combination with a propylene copolymer as described herein,include a variety of propylene homopolymers such as those having meltflow rates (MFR) from about 1 to about 20 as determined by ASTM TestD1238, condition L. Propylene homopolymers having MFRs of at least about4 (preferably at least about 8) are particularly useful and providefilms having improved die-cuttability. Useful propylene homopolymersalso may be characterized as having densities in the range of about 0.88to about 0.92 g/cm³.

[0018] A number of useful propylene homopolymers are availablecommercially from a variety of sources. Some of the useful homopolymersare listed and described in the following Table II. TABLE II CommercialPropylene Homopolymers Commercial Melt Flow Designation Company g/10 minDensity (g/cm³) WRD5-1057 Union Carbide 12.0 0.90 DX5E66 Union Carbide8.8 0.90 5A97 Union Carbide 3.9 0.90 5E98 Union Carbide 3.2 0.90 Z9470Fina 5.0 0.89 Z9470HB Fina 5.0 0.89 Z9550 Fina 10.0 0.89 6671XBB Fina11.0 0.89 3576X Fina 9.0 0.89 3272 Fina 1.8 0.89 SF6100 Montell 11.00.90

[0019] The propylene copolymers which may be utilized generally comprisecopolymers of propylene and up to about 40% by weight of at least onealpha-olefin selected from ethylene and alpha-olefins containing from 4to about 8 carbon atoms. Examples of useful alpha-olefins includeethylene, 1-butene, 1-pentene, 4-methyl-1-pentene, 1-hexene, 1-heptene,and 1-octene. More often, the copolymers of propylene which are utilizedin the present invention comprise copolymers of propylene with ethylene,1 -butene or 1-octene. The propylene alpha-olefin copolymers useful inthe present invention include random as well as block copolymersalthough the random copolymers generally are preferred. Blends of thecopolymers as well as blends of the copolymers with propylenehomopolymers can be utilized as the composition for the base layer. Inone preferred embodiment, the propylene copolymers arepropylene-ethylene copolymers with ethylenic contents of from about 0.2%to about 10% by weight. Preferably, the ethylene content is from about3% to about 10% by weight and more preferably from about 3% to about 6%by weight. With regard to the propylene-1-butene copolymers, 1-butenecontents of up to about 15% by weight are useful. In one embodiment, the1-butene content generally may range from about 3% by weight up to about15% by weight, and in other embodiments, the range may be from about 5%to about 15% by weight. Propylene-1-octene copolymers useful in thepresent invention may contain up to about 40% by weight of 1-octene.More often, the propylene-1-octene copolymers will contain up to about20% by weight of 1-octene.

[0020] The propylene copolymers useful in the present invention may beprepared by techniques well known to those skilled in the art, and manysuch copolymers are available commercially. For example, the copolymersuseful in the present invention may be obtained by copolymerization ofpropylene with an alpha-olefin such as ethylene or 1-butene usingsingle-site metallocene catalysts. A list of some useful commerciallyavailable propylene copolymers is found in the following Table III. Thepropylene copolymers useful in the invention have an MFR of from about 1to about 20, preferably from about 1 to about 12. TABLE III CommercialPropylene Copolymers Commer- Melt Flow cial % Eth- % Rate Density NameSource ylene 1-Butene (g/10 mins) (g/cm³) DS4D05 Union Carbide — 14 6.50.890 DS6D20 Union Carbide 3.2 — 1.9 0.890 DS6D81 Union Carbide 5.5 —5.0 0.900 SRD4-127 Union Carbide —  8 8.0 NA SRD4-104 Union Carbide — 115.0 NA SRD4-105 Union Carbide — 14 5.0 NA

[0021] The monolayer films of the invention which are described abovealso are characterized as being free of copolymers of ethylene monomerwith an ethylenically unsaturated carboxylic acid or ester comonomer. Afilm is considered to be free of such copolymers when there is less thanabout 0.1% by weight of such copolymers in the film. Specific examplesof copolymers which are excluded from the films of this embodiment ofthe invention are the ethylene-vinyl acetate (EVA), ethylene methylacrylate (EMA) and ethylene n-butyl acrylate (EnBA) copolymers.

[0022] Although the films of the invention may contain other polymersand copolymers, the presence of incompatible polymers and copolymersshould be minimized or essentially avoided when a clear film (low haze)is desired. The amount of incompatible polymer which can be includeddepends on the particular polymer (e.g., degree of incompatibility) andthe degree of haze that can be tolerated.

[0023] Various nucleating agents and particulate fillers can beincorporated into the monolayer films of the present invention. Theamount of nucleating agent added should be an amount sufficient toprovide the desired modification of the crystal structure while nothaving an adverse effect on the desired properties of the films. It isgenerally desired to utilize a nucleating agent to modify the crystalstructure and provide a large number of considerably smaller crystals orspherulites to improve the transparency (clarity), stiffness, and thedie-cuttability of the film. Obviously, the amount of nucleating agentadded to the film formulation should not have a deleterious effect onthe clarity of the film. Nucleating agents which have been usedheretofore for polymer films include mineral nucleating agents andorganic nucleating agents. Examples of mineral nucleating agents includecarbon black, silica, kaolin and talc. Among the organic nucleatingagents which have been suggested as useful in polyolefin films includesalts of aliphatic mono-basic or di-basic acids or arylalkyl acids suchas sodium succinate, sodium glutarate, sodium caproate, sodium4-methylvalerate, aluminum phenyl acetate, and sodium cinnamate. Alkalimetal and aluminum salts of aromatic and alicyclic carboxylic acids suchas aluminum benzoate, sodium or potassium benzoate, sodiumbeta-naphtholate, lithium benzoate and aluminum tertiary-butyl benzoatealso are useful organic nucleating agents. Substituted sorbitolderivatives such as bis (benzylidene) and bis (alkylbenzilidine)sorbitols wherein the alkyl groups contain from about 2 to about 18carbon atoms are useful nucleating agents. More particularly, sorbitolderivatives such as 1,3,2,4-dibenzylidene sorbitol,1,3,2,4-di-para-methylbenzylidene sorbitol, and1,3,2,4-di-para-methylbenzylidene sorbitol are effective nucleatingagents for polypropylenes. Useful nucleating agents are commerciallyavailable from a number of sources. Millad 8C-41-10 is a concentrate of10% Millad 3988 (a sorbitol nucleating agent) and 90% polypropylene andis available from Milliken Chemical Co.

[0024] When a nucleating agent is incorporated into the film, theamounts of nucleating agent incorporated into the film formulations ofthe present invention are generally quite small and range from about 100to about 2000 or 4000 ppm of the film. Preferably the amount ofnucleating agent should not exceed about 2000 ppm, and in oneembodiment, a concentration of about 300 to 500 ppm appears optimum.

[0025] The film may contain other additives and particulate fillers tomodify the properties of the film. For example, colorants may beincluded in the film such as TiO₂, CaCO₃, etc. The presence of smallamounts of TiO₂, for example, results in a white facestock. Antiblockagents also can be included in the base layer. AB-5 is an antiblockconcentrate available from A. Schulman Inc., 3550 West Market Street,Akron, Ohio 44333, which comprises 5% solid synthetic amorphous silicain 95% low density polyethylene. ABPPO5SC is an antiblock concentratefrom Schulman containing 5% of the synthetic amorphous silica in apropylene copolymer. The amount of antiblock agent (silica) present inthe base layer may range from about 500 to about 5000 ppm, with amountsof about 1000 ppm being preferred.

[0026] In some embodiments, particularly where it is desired that thefilm be clear, the film is free of inert particulate filler materialalthough very small amounts of particulate filler material may bepresent in the film due to impurities etc. The term “free of” isintended to mean that the film contains less than about 0.1 % by weightof particulate filler material. Films which are free of particulatefiller are particularly useful when it is desired to prepare a filmwhich is clear which may be characterized as having low haze, forexample, less than 10%, or less than 6% haze, or in some instances lessthan about 2%. Haze or clarity is determined using a BYK-Gardner haze-10gloss meter as known in the art. It has been observed that the biaxiallystretch-oriented films of this invention which are free of fillerparticles exhibit improved clarity, and in some instances, the films arecrystal clear. As noted above, incompatible polymers and copolymers areabsent or present in minor amounts when clear films are desired.

[0027] The monolayer films of the present invention can be formed by avariety of techniques known to those skilled in the art including blownor cast extrusion, extrusion coating or by a combination of thesetechniques.

[0028] The films of the present invention, as noted above, are biaxiallystretch-oriented. Simultaneous biaxial orientation or sequential biaxialorientation may be utilized in preparing the films of the presentinvention. One preferred process is to produce the monolayer films bysimultaneous biaxial orientation processes.

[0029] Although it is possible to prepare the desired die-cuttable,biaxially stretch-oriented monolayer films of the present invention bystretching the film in the machine direction (MD) in an amount which isequal to or greater than the stretching in the cross direction (CD), inone embodiment, it is preferred that the stretch orientation in the MDbe greater than the orientation in the CD by at least about 10%, or evenby 20%. The orientation in the MD may be at a stretch ratio of fromabout 3:1 to about 10:1 or higher although more often the stretch ratioin the MD is from about 5:1 to about 10:1. In other embodiments, thestretch ratio in the MD may range of from about 9:1 to about 10:1 orhigher. As mentioned above, the stretch ratio in the CD often is lessthan the stretch orientation in the MD. Thus, stretch ratios in the CDmay be from greater than 1:1 to about 5:1, or from greater than 1:1 toabout 3:1 or greater than 1:1 to about 2:1. In a particular example ofthis latter embodiment, a monolayer film of a polyolefinstretch-oriented in the MD at a ratio of 9:1 to 10:1 is stretch orientedin the CD at a ratio of from greater than 1:1 to about 2:1 or 3:1 or4:1. The polyolefins which may be utilized in this embodiment includepolyethylenes, polypropylenes, copolymers of propylene and up to about40% by weight of at least one alpha-olefin selected from ethylene andalpha-olefins containing from 4 to about 8 carbon atoms as describedabove, and mixtures thereof. Thus, in this particular embodiment, thepolyolefins include low density polyethylene, medium densitypolyethylene and high density polyethylene, although the low and mediumdensity polyethylenes are more often utilized. The high densitypolyethylenes are those having a density of greater than about 0.940 toabout 0.965 g/cm³.

[0030] The monolayer films of the invention are biaxially oriented byhot stretching the films at a temperature equal to or above thesoftening temperature of the film. The temperatures utilized in thehot-stretching step will depend, among other things, on the filmcomposition and whether any nucleating agents are present. Whensequential orientation is utilized, the temperature for the MDstretching may not be the same as the temperature for the CD stretching.Generally, the MD orientation is conducted at a lower temperature thanthe CD orientation. For example, for a propylene homopolymer, thetemperature for the MD orientation may be around 140° C. and thetemperature for the CD orientation around 1 80° C.

[0031] In one embodiment of the present invention, the monolayer filmswhich have been stretch oriented to the desired stretch ratio while in aheated condition are then passed over annealing rolls where thestretched films are annealed or heat-set. After the heat-setting orannealing operation, the film is then passed over a chill roll tocomplete the hot-stretch and heat-set operation. In another embodiment,the hot-stretched film is relaxed in both the MD and CD by from about 5to about 25%, and more often from about 10 to about 20% prior to beingsubjected to the annealing or heat setting step. The temperature used inthe hot-stretching step and the temperature utilized in the heat settingstep depends on the particular polymer utilized to form the monolayerfilm, and these temperatures may range from about 110° C. to about 180°C. The temperatures utilized for the hot-stretching and the heat settingsteps may be the same although in some instances, the temperature of theheat setting step is somewhat higher than the temperature utilized forthe hot-stretching step. Thus, the heat setting step may be conducted attemperatures of up to about 180° C. When the hot stretched films of thepresent invention are subjected to a heat setting or annealing step, thefilm generally is heat set or annealed from about 5 to about 25 seconds,and more often, from about 10 to about 20 seconds. The stretch-orientedmonolayer films of the present invention which are also heat-set orannealed are essentially devoid of “memory” of a pre-existingconfiguration to which a film tends to return under the influence ofheat.

[0032] That is, the heat-set and annealed films of the present inventiondo not have a tendency to shrink or distort when subsequently subjectedto an elevated temperature.

[0033] The thickness of the monolayer films described above may rangefrom about 0.5 mils (12.5 microns) to about 6 mils (150 microns)depending upon the anticipated utility of the film. More often, however,the biaxially stretch-oriented monolayer films of this invention have athickness of from about 1 mil to about 3.5 or 4 mils. In one embodiment,the film thickness will range from about 2 to about 2.5 mils.

[0034] The biaxially stretch-oriented monolayer films of the presentinvention which have been described above exhibit stiffnesscharacteristics which enable the films to be utilized in applicationssuch as die-cuttable labelstock. Thus, the Gurley stiffness of thebiaxially stretch-oriented monolayer films of the present invention mayrange from about 3 to about 50, more often from about 5 or 10 up toabout 50 in the machine direction. The Gurley stiffness of the monolayerfilms of the invention in the cross direction will generally be lessthan the Gurley stiffness in the machine direction. The Gurley stiffnessof the monolayer films of the present invention is measured inaccordance with the TAPPI Gurley Stiffness Test T543pm.

[0035] As mentioned above, the films of the present invention also maycomprise die-cuttable, stretch-oriented multilayer films which comprise

[0036] (A) a base layer having an upper surface and a lower surface, andcomprising polyethylene having a density of about 0.940 g/cm³ or less, apropylene homopolymer or copolymer, or mixtures thereof wherein the baselayer is free of copolymers of ethylene with an ethylenicallyunsaturated carboxylic acid or ester, and

[0037] (B) a first skin layer of a thermoplastic polymer bonded to theupper surface of the base layer, wherein the tensile modulus of themultilayer film in the machine direction is greater than the tensilemodulus in the cross direction, and the tensile modulus in the crossdirection is about 150,000 psi or less.

[0038] Any of the monolayer films described above, prior to orientation,may be utilized as the base layer of the multilayer film. That is, thebase layer of the multilayer films of the present invention may compriseany of the polyethylenes described above, any of the propylenehomopolymers or copolymers described above, or mixtures thereof andwherein the base layer is free of copolymers of ethylene with anethylenically unsaturated carboxylic acid or ester. The base layer alsomay contain any of the ingredients described above as being optional inthe monolayer films such as fillers, colorants, nucleating agents,antiblock agents, etc. If a clear multilayer film is desired, the baselayer will be free of inert particulate filler. If an opaque multilayerfilm is desired, the base layer may contain particulate fillers asdescribed above.

[0039] The first skin layer may comprise any other variety ofthermoplastic polymers. Examples of thermoplastic polymers andcopolymers useful as the first skin layer of the multilayer filmcompositions of the present invention include polyolefins, polyamides,polystyrene, polystyrene-butadiene, polyester, polyester copolymer,polyurethane, polysulfone, polyvinylidene chloride, styrene-maleicanhydride copolymer, styrene acrylonitrile copolymer, ionomer based onsodium or zinc salts of ethylene methacrylic acid, polymethylmethacrylate, cellulosic, fluoroplastic, acrylic polymer and copolymer,polycarbonate, polyacrylonitrile, ethylene-vinyl acetate copolymer, andmixtures thereof. The composition of the first skin layer is a matter ofchoice depending on the properties desired for the first skin layer suchas costs, weatherability, printability, etc.

[0040] The first skin layer may, and often does contain mixtures ofpolyolefins (e.g., polyethylene, propylene polymers and copolymers) anda copolymer of ethylene with an ethylenically unsaturated carboxylicacid or ester comonomer such as EVA. For example one useful skincomposition comprises a 50:50 mixture of polypropylene and EVA.

[0041] The first skin layer may also contain other additives such asparticulate fillers, antiblock agents, nucleating agents, etc., asdescribed above. When a clear multilayer film is desired, the first skinlayer (as well as the base layer), generally will be free of particulatefiller material. When an opaque film is desired, the skin layer (and/orthe base layer) will contain particulate filler material. Thus, it ispossible to prepare the multilayer films of this invention ranging fromopaque films to clear films, and the clear films may be characterized ashaving a haze of less than 10%, or less than 6%, or even less than about2%.

[0042] In yet another embodiment of the present invention, themultilayer films described above comprising a base layer having an uppersurface and a lower surface, and a first skin layer of a thermoplasticpolymer bonded to the upper surface of the base layer, may also containa second skin layer bonded to the lower surface of the base layer wherethe second skin layer may comprise any of the thermoplastic polymersdescribed above as being useful in the first skin layer, and thecomposition of the second skin layer may be the same as or differentfrom the composition of the first skin layer. Generally, the two skinlayers are different since the properties desired for these layers aredifferent. Printability, weatherability, etc. are desired for the firstskin layer whereas other properties such as good bonding to an adhesivelayer may be desired for the second skin layer.

[0043] The multilayer films of the present invention may be prepared bya variety of techniques known to those skilled in the art includingblown or cast extrusion, or extrusion coating or by a combination ofthese techniques. U.S. Pat. No. 5,186,782 (Freedman), and U.S. Pat. Nos.5,242,650 (Rackovan et al) and 5,435,963 (Rackovan et al) discloseuseful procedures for preparing multilayer films, and these patents arehereby incorporated by reference. The multilayers can be formed bysimultaneous extrusion from a suitable known type of coextrusion die,and the layers are adhered to each other in a permanently combined stateto provide a unitary coextrudate. Alternatively, the base layer can beformed by extrusion of the base layer on a substrate followed byextrusion coating of the first skin layer (and optionally the secondskin layer) onto the base layer thereby forming a two or three layerstructure wherein the layers are adhered to each other in a permanentlycombined state. In another alternative embodiment, the two or threelayers may be separately formed by extrusion and thereafter laminatedtogether by the application of heat and pressure.

[0044] Generally, the base layer is relatively thick compared to thefirst skin layer and the second skin layer. In another, althoughgenerally not preferred embodiment, the first skin layer may berelatively thick compared to the base layer. Accordingly, thicknessratios for the three layered films may range from about 90:5:5 to5:5:90. However, generally preferred thickness ratios for the threelayered films (base: first skin:second skin) include 90:5:5, 80:10:10,70:15:15, 85:5:10, and 80:5:15.

[0045] The multilayer films of the present invention, as noted above,are biaxially stretch-oriented. Simultaneous biaxial orientation orsequential biaxial orientation may be utilized in preparing themultilayer films of the present invention. Simultaneous biaxialorientation of the multilayer films of the present invention is apreferred process in one embodiment of the present invention.

[0046] Although in some instances, it is possible to prepare the desireddie-cuttable, biaxially stretch-oriented multilayer films of the presentinvention by stretching the film in the machine direction (MD) in anamount which is equal to or greater than the stretching in the crossdirection (CD), the stretch orientation in the MD more often will begreater than the orientation in the CD by at least about 10%, or even by20%. The orientation in the MD may be at a stretch ratio of from about3:1 to about 10:1 or higher although a preferred stretch ratio in the MDis from about 5:1 to about 10:1. In other embodiments, the stretch ratioin the MD is within the range of from about 9:1 to about 10:1 or higher.As mentioned above, the stretch ratio in the CD generally is less thanthe stretch orientation in the MD. Thus, stretch ratios in the CD arefrom greater than 1:1 to about 5:1, or from greater than 1:1 to about3:1 or greater than 1:1 to about 2:1.

[0047] The thickness of the multilayer films described above will rangefrom about 0.5 mils (12.5 microns) to about 6 mils (150 microns)depending upon the anticipated utility of the film. More often, however,the multilayer films of the present invention will have a thickness ofabout 1 to about 3.5 or 4 mils or from about 2 to about 3 mils. Suchthicknesses are particularly useful for preparing labels to be appliedto rigid and flexible substrates. As noted earlier, a particular featureof the multilayer film facestocks of the invention is that very thinfilms (i.e., 1 to 3 mils) can be prepared that are useful in forminglabels.

[0048] The selection of a particular polymer for the second skin layeris dependent on the properties and characteristics which are to be addedby the presence of the second skin layer. The polymer for the secondskin layer should be compatible with the polymer of the base layer toprovide sufficient adhesion to the base layer. For example, if the baselayer contains a propylene polymer, a second skin layer comprising atleast some propylene polymer will adhere to the base layer without anintermediate tie layer. It also has been discovered that the use of acomposition in the second skin layer that is different from thecomposition of the first skin layer reduces the blocking tendency whenthe facestock is rolled on itself.

[0049] In one embodiment, it is preferred that the second skin layercomprise a polymer that is softer than the propylene polymer orcopolymer, or blends of propylene polymers and copolymers used in thebase layer, particularly when the second skin layer is joined with anadhesive to a release coated liner. In particular, it is preferred thatthe material of the second skin layer has a lower tensile modulus thanthe tensile modulus of the material comprising the base layer. The useof a lower tensile modulus second skin layer results in a facestockexhibiting improved die-cuttability when compared to a facestock whereinthe material of the second skin layer has a higher tensile modulus thanthe material of the base layer.

[0050] The stiffness of the multilayer films of the present invention isimportant for proper dispensing of labels over a peel plate at higherline speeds. Biaxial orientation of the multilayer films increases thetensile modulus in the machine direction and cross direction. Theincrease in the machine direction contributes to dimensional stabilityand good print registration.

[0051] The stiffness of the oriented multilayer films in the machinedirection generally should be at least about 2 or 3, and may be as highas 50 or 60 Gurley. More often the stiffness of the oriented multilayerfilms in the MD is in the range of from about 5 or 10 up to about 25 or35 Gurley as measured in accordance with the TAPPI Gurley Stiffness TestT543pm. The Gurley stiffness in the CD generally is in the same rangesbut the stiffness in the CD is less than the stiffness in the MD.

[0052] The biaxially stretch-oriented monolayer films and multilayerfilms of the present invention which have been described above arefurther characterized as having a tensile modulus in the cross directionof about 150,000 psi or less. The tensile modulus of the films can bedetermined in accordance with ASTM Test D882 entitled “TensileProperties of Thin Plastic Sheeting”. In one embodiment of theinvention, the tensile modulus of the films of the present invention inthe cross direction is less than the tensile modulus of the films in themachine direction. Labels prepared from such films are observed toexhibit improved conformability. Thus, in one embodiment, the tensilemodulus of the films of the present invention in the machine directionmay be as high as 200,000 psi or even as high as 250,000 psi, and thetensile modulus in the cross direction is 150,000 psi or less. In otherembodiments, the tensile modulus in the machine direction is 150,000 orless or even 125,000 or less, and the tensile modulus in the crossdirection is less than 100,000 psi.

[0053] The following Examples identified in Table IV illustrate themonolayer films of the present invention. Unless otherwise indicated inthe following Examples and elsewhere in the specification and claims,all parts and percentages are by weight, temperatures are in degreescentigrade, and pressures are at or near atmospheric pressure.

[0054] The films in the following Table IV are prepared by extruding themelted charges through an extrusion die and casting on cooling rolls.The extrudate is in the form of sheets which are cut to 10×10 cm² andsubsequently biaxially hot-stretched on a laboratory film stretcher atthe ratios specified in Table IV at a draw rate of 400%/second. Thestretcher is a type KARO IV stretcher manufactured by BrücknerMaschinenbau. The oriented films are relaxed and annealed (heat set) asset forth in Table IV. Some of the properties of the monolayer films ofExamples 1-11 are reported in Table V. TABLE IV BiaxiallyStretch-Oriented Monolayer Films Film Stretch Ratio OrientationRelaxation Anneal Thickness Example Composition MD CD Temp (° C.) %¹Period (sec.)² (Mils) 1 11G1 7:1 5:1 122 10 20 2.26 2 11G1 8:1 5:1 11810 20 1.82 3 11G1 8:1 5:1 122 10 20 1.40 4 6D81 5:1 5:1 122 10 20 3.28 56D81 8:1 4:1 130 10 20 2.58 6 6D81 9:1 4:1 130 10 20 2.30 7 DS4DO5 8:14:1 130 10 20 2.46 8 DS4DO5 10:1  2.5:1   130 10 20 3.24 9 DS4DO5 10:1 4:1 130 10 20 2.16 10 5E98 + 2% NA³ 10:1  2.5:1   160 10 10 2.86 11DS5E98 10:1  2.5:1   160 10 10 2.07

[0055] TABLE V Properties of Biaxially Stretch-Oriented Monolayer Films2% Secant Thickness Gurley Stiffness Modulus (psi) Haze Example (Mils)MD CD MD CD (%) 1 2.26 7.0 5.8 63,600 33,100 1.7 2 1.82 3.9 3.4 42,20028,500 2.1 3 1.40 1.7 1.6 42,200 32,700 4.6 4 3.28 28.3 27.2 73,30072,800 1.1 5 2.58 15.2 10.1 80,000 74,700 1.3 6 2.30 11.8 7.2 89,10067,800 1.3 7 2.46 16.6 12.6 113,300  87,800 0.9 8 3.24 43.6 29.6152,000  93,300 0.9 9 2.16 12.8 7.2 134,500  99,800 0.7 10 2.86 51.932.4 234,300  149,400  4.9 11 2.07 18.6 11.3 235,600  145,500  5.2

[0056] The following Examples 12-14 illustrate the multilayer films ofthe invention. The multilayer films are prepared by coextrusion asdescribed above. The films are biaxially oriented at the ratios and atthe temperatures shown in Table VI. The draw rate is 400%/second. Someof the properties of the films of Examples 12-14 are reported in TableVII. TABLE VI Biaxially Stretch-Oriented Multilayer Films OverallStretch Base Skin Thickness Ratio Orientation Relaxation Anneal PeriodExample Layer Layer (Mils) MD CD Temp (° C.) (%)¹ (Sec)² 12 11G1 20272.14 7:1 5:1 118 10 20 13 11G1 2027 2.52 8:1 4:1 130 10 20 14 6D81 50%5E98 2.76 8:1 4:1 130 10 20 50% EVA*

[0057] TABLE VII Properties of Biaxially Stretch-Oriented MultilayerFilms Overall 2% Secant Thickness Gurley Stiffness Modulus (psi) Example(Mils) MD CD MD CD Haze (%) 12 2.14 4.8 4.4 43,700 33,600 2.6 13 2.5217.4 11.3 86,900 71,100 5.6 14 2.76 16.8 12.2 73,000 63,000 71.1

[0058] The die-cuttability of the biaxially oriented films of Examples 1-14 is evaluated by die-cutting shapes in the films and thereaftermeasuring the friction energy required to separate the matrix from thedie-cut shape. A low friction energy value (e.g., about 150 g-cm orless) indicates the film exhibits good die-cuttability. Friction energyvalues of less than 120 and even less than 100 are particularlydesirable. This test which is conducted as follows is described in moredetail in U.S. Pat. No. 5,961,766 entitled “Method For Selecting ASubstrate Intended For Use In A Cutting Operation”, which patent ishereby incorporated by reference.

[0059] A test sheet of each film having the dimensions of 7×10″(17.8×25.4 cm) and a paper liner are advanced through a die-cutter where10 shapes are cut in the film but not the liner. The die-cutter has acylindrical profile. The die-cutting roll has a diameter of 3 inches(76.2 mm), with one cavity across and 10 cavities around. Each of thecavities are 6 inches (152.4 mm) long (or across), {fraction (15/16)}inch (22.25 mm) wide (or deep) and have rounded corners with diametersof {fraction (3/32)} inch (2.38 mm). The separation between adjacentcavities is ⅛ inch (3.175 mm). The anvil roll has a diameter of 5 inches(127 mm). The gap between the anvil and the tip of the die is 2.2 mils(0.0559 mm). The die pressure is 300 psi (208500 kg/m²), and the speedof the die is 15 m/min.

[0060] The die-cut in each test sheet is deep enough to penetrate thefilm but not the liner. The shapes that are formed are rectangular andarranged side-by-side on the test sheet, one shape across and ten deep.The long dimension of each shape is parallel to the long dimension ofthe next adjacent shape. The shapes have the dimensions of ⅞×6″ (22.25mm×1 52.4 mm) and are equidistant from each other. The gap between eachshape is ⅛ inch (3.175 mm). A matrix, which consists of the portion ofthe waste facestock around the shapes, is also formed during thedie-cutting.

[0061] A test sample is formed by cutting the die-cut test sheet alongthe center line of the long dimension of one shape and then along thecenter line of the long dimension of the next adjacent shape. The cutsare parallel to each other. Each test sample consists of one-half of oneshape, one-half of the next adjacent shape, the matrix around the shapeportions.

[0062] The friction energy required to separate the matrix from thedie-cut shapes of each sample is measured using a modified TA-XT2Texture Analyzer provided by Stable Micro Systems, Unit 105, BlackdownRural Industries, Haste Hill, Haslemere, Surrey GU 27 3AY, England. TheTA-XT2 Texture Analyzer is a tensile testing device. It is modified asfollows: the fixture on the top crosshead is removed and substituted byan upper L-shaped bracket; one arm of the upper L-shaped bracket isattached to the upper frame; the platform mounted on the base is removedand substituted by a lower L-shaped bracket. Each test sample is testedby attaching an edge of the matrix of the test sample to the upperL-shaped bracket, and attaching the edge of each shape portion adjacentto the attached matrix edge to the lower L-shaped bracket. The textureanalyzer is activated and the matrix is separated from the shapeportions at a rate of 5 mm/s.

[0063] The force used to separate the matrix and the displacement ofthis force along the length of the test sample during separating isplotted using software provided with the TA-XT2 Texture Analyzer. Thearea under the plot is also determined using software provided with theTA-XT2 Texture Analyzer. The area under the plot has the units ofgram-seconds. The result is multiplied by the stripping speed (5 mm/s)and after making appropriate corrections for units (i.e., mm to cm), thefriction energy results are provided in terms of gram-centimeters(g-cm). Higher friction energy numbers are associated with poorly cutfacestocks or adhesive flowback. The test results for the films ofExamples 1-14 are summarized in Table VIII. For each film, about seventest samples are tested and the averages for these test samples aregiven in Table VIII. TABLE VIII Friction Energy Test Results Film ofFriction Energy Example (g-cm) 1 68 2 93 3 109 4 54 5 51 6 41 7 74 8 859 43 10 40 11 65 12 57 13 54 14 36

[0064] In another embodiment of the present invention, the biaxiallyoriented monolayer or multilayer films of the present invention may beutilized for preparing labeistock for adhesive labels. The labelstockcomprises the monolayer film or the multilayer film described above, andan adhesive layer which is adhesively joined to one surface of the film.

[0065] In one embodiment, an adhesive containing labelstock used inadhesive labels comprises

[0066] (A) a die-cuttable, biaxially oriented multilayer film comprising

[0067] (A-1) a base layer having an upper surface and a lower surface,and comprising polyethylene having a density of about 0.940 g/cm³ orless, a propylene polymer or copolymer, or mixtures thereof wherein thebase layer is free of copolymers of ethylene with an ethylenicallyunsaturated carboxylic acid or ester, and

[0068] (A-2) a first skin layer of a thermoplastic polymer bonded to theupper surface of the base layer, wherein the tensile modulus of themultilayer film in the machine direction is greater than the tensilemodulus in the cross direction, and the tensile modulus of themultilayer film in the cross direction is 150,000 psi or less, and

[0069] (B) an adhesive layer having an upper surface and a lower surfacewherein the upper surface of the adhesive layer is adhesively joined tothe lower surface of the base layer.

[0070] The multilayer film useful in such labelstock is described indetail above. The adhesive layer in this embodiment is adhesively joinedto the lower surface of the base layer. Additionally, the biaxiallyoriented multilayer film (A) may comprise (A-3) a second skin layerbonded to the lower surface of the base layer, and thus, the second skinlayer is between the base layer and the adhesive layer. The second skinlayers as described above can be utilized.

[0071] The adhesive layer may be directly coated on the lower surface ofthe base layer, or to the second skin layer when present, or theadhesive may be transferred from a liner with which the multilayer filmis combined. Typically, the adhesive layer has a thickness in the rangeof from about 0.1 to about 2 mils (2.5 to 50 microns). Adhesivessuitable for use in labelstocks of the present invention are commonlyavailable in the art. Generally, these adhesives includepressure-sensitive adhesives, heat-activated adhesives, hot meltadhesives, and the like. Pressure-sensitive adhesives are particularlypreferred. These include acrylic adhesives as well as other elastomerssuch as natural rubber or synthetic rubbers containing polymers orcopolymers of styrene, butadiene, acrylonitrile, isoprene andisobutylene. Pressure-sensitive adhesives are well known in the art andany of the known adhesives can be used with the facestocks of thepresent invention. In one preferred embodiment, the pressure-sensitiveadhesives are based on copolymers of acrylic acid esters, such as, forexample, 2-ethyl hexyl acrylate, with polar comonomers such as acrylicacid.

[0072] In the manufacture of labeistock from the above-describedmonolayer and multilayer films in accordance with the invention, lineror carrier stock may be provided. The liner or carrier stock maycomprise a multilayer liner made for example as disclosed in U.S. Pat.No. 4,713,273, the disclosure which is incorporated herein by reference,or may be a conventional liner or carrier consisting of a single paperof film layer which may be supplied in roll form. If it has not beenpreviously provided with a release coating and does not itself includecomponents to inherently generate a release surface at itsadhesive-contacting face, the liner or carrier may be coated with arelease coating (e.g., a silicone). If a release coating is applied, itis dried or cured following application by any suitable means.

[0073] The release face of the release liner or carrier may be coatedwith a layer of pressure-sensitive adhesive for subsequent transfer ofthe adhesive to the labelstock with which the liner or carrier isemployed. When the labelstock is combined with the liner or carrier, theadhesive is joined to the biaxially oriented film. Later, the liner orcarrier is removed to expose the adhesive, and the adhesive remainspermanently joined to the biaxially oriented film.

[0074] In some applications, the adhesive layer may be a heat-activatedadhesive or a hot-melt adhesive such as used in in-mold labelapplications, as distinguished from a pressure-sensitive adhesive. Ifthe adhesive is a heat-activated adhesive or a hot-melt adhesive, theremay be no need for the provision of a release liner for inherentreleasability such as is required when using a pressure-sensitiveadhesive.

[0075] The manufacture of pressure-sensitive adhesive labelstock fromthe above-described biaxially oriented films in accordance with theinvention is illustrated as follows. The liner or carrier stock maycomprise a multilayer liner or a conventional liner or carrierconsisting of a single paper or film layer having a release coatingwhich may be supplied in roll form. The release face of the releaseliner or carrier may be coated with a layer of pressure-sensitiveadhesive for subsequent transfer of the adhesive to the oriented filmwith which the liner or carrier is employed. When the film is combinedwith the liner or carrier, the adhesive is joined to the film. Later,the liner or carrier is removed to expose the adhesive, which nowremains permanently joined to the biaxially oriented film.

[0076] The biaxially oriented film may be printed prior to being die-cutinto individual labels. The printing step may occur before or after thecombining of liner and oriented film, but will precede the die-cuttingof the labelstock into individual labels. The film must remain inaccurate register between printing steps (for example, betweensuccessive impressions in different colors) in order that image or textbe of high quality, and between printing and subsequent die-cutting inorder that image or text be located properly on the labels. The film isunder tension during printing, and may be subjected to some increase intemperature, as for example when UV inks are cured, and the film mustmaintain dimensional stability in the machine-direction.

[0077] As noted earlier, the biaxially stretch-oriented films of thisinvention are die-cuttable, and the labelstock on a liner may be die-cutinto a series of spaced pressure-sensitive labels carried by the releaseliner or carrier. This step may be performed by cutting dies (e.g.,rotary cutting dies) in a well-known manner and involves the subsequentstripping of the ladder-shaped matrix of waste or trim surrounding theformed labels when they are die-cut (the “rungs” of the ladderrepresenting the spacing between successive labels). The labels thenremain on the liner in spaced relation with each other. One failure modein this operation involves poorly die-cut labels remaining with thematrix as it is stripped. In this mode, as release levels decrease, poordie-cutting is more likely to cause labels to stay attached to thematrix material and be removed from the liner during matrix strippingalong with the matrix. Another failure mode occurs when the die-cut goesthrough the adhesive and part of the liner leaving an impression in theliner. Another failure mode results when the films being die-cut are ofinsufficient strength. As the strength of the matrix material decreases,the matrix tends to tear as the matrix around the die-cut labels ispulled from the liner. The films of the present invention havesufficient strength to avoid or reduce breakage of the matrix onstripping.

[0078] The die-cut labels on the liner or carrier can be dispensed andapplied to various substrates by techniques known to those skilled inthe art. For example, the labels can be dispensed and applied to passingworkpieces by use of a peel-back edge to dispense the labels byprogressively removing the liner or carrier from them to thereby exposethe adhesive side of the labels and project the labels into contact withpassing workpieces. In the context of the present invention, theworkpieces may constitute substrates such as glass bottles or otherrigid articles tending to have irregularities in the surface andtherefore requiring labels that are flexible and that closely adhere(conform) to the surface without bridging local surface depressions. Thesubstrates also may be flexible plastic containers.

[0079] While the invention has been explained in relation to itspreferred embodiments, it is to be understood that various modificationsthereof will become apparent to those skilled in the art upon readingthe specification. Therefore, it is to be understood that the inventiondisclosed herein is intended to cover such modifications as fall withinthe scope of the appended claims.

1. A die-cuttable, biaxially stretch-oriented monolayer film comprisinga polyethylene having a density of about 0.940 g/cm³ or less, apropylene polymer or copolymer, or mixtures thereof, wherein the tensilemodulus of the film in the machine direction is greater than the tensilemodulus in the cross direction, the tensile modulus of the film in thecross direction is about 150,000 psi or less, and the film is free ofcopolymers of ethylene with an ethylenically unsaturated carboxylic acidor ester.
 2. The film of claim 1 comprising a propylene copolymer. 3.The film of claim 2 wherein the propylene copolymer is a copolymer ofpropylene and up to about 40% by weight of at least one α-olefinselected from ethylene and α-olefins containing from 4 to about 8 carbonatoms.
 4. The film of claim 3 wherein the α-olefin is ethylene or 1-butene.
 5. The film of claim 1 comprising a polyethylene having adensity of from about 0.890 to about 0.925 g/cm³ .
 6. The film of claim1 which is free of inert particulate filler.
 7. The film of claim 1containing inert particulate filler.
 8. The film of claim 1 having ahaze of less than about 10%:
 9. The film of claim 1 having a haze ofless than about 6%.
 10. The film of claim 1 having a haze of less thanabout 2%.
 11. The film of claim 1 wherein the stretch-orientation in themachine direction is greater than the orientation in the cross directionby at least about 10%.
 12. The film of claim 11 wherein the film isoriented in the machine direction at a stretch ratio of from about 5:1to about 1 0:1.
 13. The film of claim 1 wherein the film contains atleast one nucleating agent.
 14. The film of claim 1 having a Gurleystiffness in the machine direction of from about 1 0 to about
 50. 15.The film of claim 1 having a thickness of about 3.5 mils or less. 16.The film of claim 1 having a thickness of from about 2 to about 2.5mils.
 17. The film of claim 1 wherein the film has been biaxiallystretch-oriented and heat set.
 18. The film of claim 1 wherein the filmcomprises polyethylene having a density of from about 0.890 to about0.925 g/cm³.
 19. The film of claim 1 wherein the film has been orientedin the machine direction at a stretch ratio of about 9:1 to about 10:1,and oriented in the cross direction at a stretch ratio of greater than1:1 up to about 3:1.
 20. The film of claim 19 wherein the stretch ratioin the cross direction is less than about 2:1.
 21. The film of claim 1having a friction energy of less than about 120 g-cm.
 22. Adie-cuttable, biaxially stretch-oriented monolayer film comprisingpolyethylene having a density of 0.940 g/cm³ or less, a propylenepolymer or copolymer, or mixtures thereof wherein the stretchorientation of the film in the machine direction is greater than thestretch orientation in the cross direction by at least 10%, the tensilemodulus of the film in the cross direction is 150,000 psi or less, andthe film is free of copolymers of ethylene with an ethylenicallyunsaturated carboxylic acid or ester.
 23. The film of claim 22 whereinthe stretch-orientation in the machine direction is greater than thestretch-orientation in the cross direction by at least about 20%. 24.The film of claim 22 wherein the film has been stretched in the machinedirection at a ratio of from about 5:1 to about 10:1.
 25. The film ofclaim 22 comprising a polyethylene having a density of from about 0.890to about 0.925 g/cm³.
 26. The film of claim 22 comprising a copolymer ofpropylene and up to about 40% by weight of at least one olefin selectedfrom ethylene and α-olefins containing from 4 to about 8 carbon atoms.27. The film of claim 22 wherein the film has been stretch oriented inthe machine direction at a ratio of from about 9:1 to about 10:1, and inthe cross direction at a ratio of greater than 1:1 to about 3:1.
 28. Adie-cuttable, stretch-oriented multilayer film comprising (A) a baselayer having an upper surface and a lower surface, and comprisingpolyethylene having a density of about 0.940 g/cm³ or less, a propylenehomopolymer or copolymer, or mixtures thereof wherein the base layer isfree of copolymers of ethylene with an ethylenically unsaturatedcarboxylic acid or ester, and (B) a first skin layer of a thermoplasticpolymer bonded to the upper surface of the base layer, wherein thetensile modulus of the multilayer film in the machine direction isgreater than the tensile modulus in the cross direction, and the tensilemodulus in the cross direction is about 150,000 psi or less.
 29. Thefilm of claim 28 wherein the base layer is free of inert particulatefiller.
 30. The multilayer film of claim 28 wherein the base layercomprises a propylene copolymer.
 31. The multilayer film of claim 28wherein the base layer comprises a propylene copolymer which is acopolymer of propylene and up to about 40% by weight of at least oneα-olefin selected from ethylene and α-olefins containing from 4 to about8 carbon atoms.
 32. The film of claim 31 wherein the α-olefin isethylene or 1 -butene.
 33. The multilayer film of claim 28 wherein thebase layer comprises polyethylene having a density of from about 0.890to about 0.925 g/cm³.
 34. The multilayer film of claim 28 wherein thefirst skin layer (B) contains inert particulate filler.
 35. Themultilayer film of claim 28 wherein the first skin layer (B) is free ofinert particulate filler.
 36. The multilayer film of claim 28 having ahaze of less than 10%.
 37. The multilayer film of claim 28 having a hazeof less than 6%.
 38. The multilayer film of claim 28 wherein the firstskin layer comprises at least one polyolefin, polyamide, polystyrene,polystyrene-butadiene, polyester, polyester copolymer, polyurethane,polysulfone, polyvinylidene chloride, styrene-maleic anhydridecopolymer, styrene acrylonitrile copolymer, ionomer based on sodium orzinc salts of ethylene methacrylic acid, polymethyl methacrylate,cellulosic, fluoroplastic, acrylic polymer and copolymer, polycarbonate,polyacrylonitrile, ethylene-vinyl acetate copolymer, and mixturesthereof.
 39. The multilayer film of claim 28 wherein the base layer andthe first skin layer are formed by coextrusion.
 40. The multilayer filmof claim 28 wherein the stretch-orientation in the machine direction isgreater than the orientation in the cross direction by at least 10%. 41.The multilayer film of claim 28 which has been oriented in the machinedirection at a stretch ratio of from about 5:1 to about 10:1.
 42. Themultilayer film of claim 28 wherein the base layer or first skin layer,or both, also contain a nucleating agent.
 43. The multilayer film ofclaim 28 containing a second skin layer bonded to the lower surface ofthe base layer.
 44. The multilayer film of claim 43 wherein thecomposition of the second skin layer is different from the compositionof the first skin layer.
 45. The multilayer film of claim 28 having aGurley stiffness in the machine direction of from about 10 to about 50.46. The multilayer film of claim 28 having an overall thickness of fromabout 2 to about 3 mils.
 47. The multilayer film of claim 28 wherein thefilm has been biaxially stretch-oriented and heat set.
 48. Themultilayer film of claim 28 wherein the multilayer film has been stretchoriented in the machine direction at a ratio of from about 9:1 to about10:1, and in the cross direction at a ratio of from greater than 1:1 toabout 3:1.
 49. The multilayer film of claim 28 having a friction energyof less than
 120. 50. The multilayer film of claim 28 having a frictionenergy of less than
 80. 51. A die-cuttable, biaxially stretch-orientedmultilayer film comprising (A) a base layer having an upper surface anda lower surface, and comprising polyethylene having a density of fromabout 0.940 g/cm³ or less, a propylene polymer or copolymer, or mixturesthereof wherein the base layer is free of copolymers of ethylene with anethylenically unsaturated carboxylic acid or ester, and (B) a first skinlayer of a thermoplastic polymer bonded to the upper surface of the baselayer, wherein the stretch-orientation of the multilayer film in themachine direction is greater than the stretch-orientation in the crossdirection by at least 10%, and the tensile modulus of the multilayerfilm in the cross direction is 150,000 psi or less.
 52. The film ofclaim 51 wherein the stretch-orientation in the machine direction isgreater than the stretch-orientation in the cross direction by at leastabout 20%.
 53. The film of claim 51 wherein the film has been stretchedin the machine direction at a ratio of from about 5:1 to about 10:1. 54.The film of claim 51 wherein the base layer comprises a copolymer ofpropylene and up to about 40% by weight of at least one α-olefinselected from ethylene and α-olefins containing from 4 to about 8 carbonatoms.
 55. The film of claim 51 wherein the base layer comprises apolyethylene having a density of from about 0.890 to about 0.925 g/cm³.56. An adhesive containing labelstock for use in adhesive labels whichcomprises (A) a die-cuttable, biaxially oriented multilayer filmcomprising (A-1) a base layer having an upper surface and a lowersurface, and comprising polyethylene having a density of about 0.940g/cm³ or less, a propylene polymer or copolymer, or mixtures thereofwherein the base layer is free of copolymers of ethylene with anethylenically unsaturated carboxylic acid or ester, and (A-2) a firstskin layer of a thermoplastic polymer bonded to the upper surface of thebase layer, wherein the tensile modulus of the multilayer film in themachine direction is greater than the tensile modulus in the crossdirection, and the tensile modulus of the multilayer film in the crossdirection is 150,000 psi or less, and (B) an adhesive layer having anupper surface and a lower surface wherein the upper surface of theadhesive layer is adhesively joined to the lower surface of the baselayer.
 57. The labelstock of claim 56 wherein the base layer comprises apropylene copolymer.
 58. The labelstock of claim 56 wherein the baselayer comprises a propylene copolymer which is a copolymer of propyleneand up to about 40% by weight of at least one α-olefin selected fromethylene and α-olefins containing from 4 to about 8 carbon atoms. 59.The labelstock of claim 58 wherein the α-olefin is ethylene or 1-butene.
 60. The labelstock of claim 56 wherein the base layer is freeof inert particulate filler.
 61. The labelstock of claim 56 wherein thebase layer comprises polyethylene having a density of from about 0.890to about 0.925 g/cm².
 62. The labelstock of claim 56 wherein themultilayer film (A) has been biaxially stretch-oriented and heat set.63. The labelstock of claim 56 wherein the multilayer film (A) has aGurley stiffness in the machine direction of from about 10 to about 50.64. The labeistock of claim 56 wherein the stretch orientation of themultilayer film (A) in the machine direction is greater than the stretchorientation in the cross direction by at least about 20%.
 65. Thelabelstock of claim 56 wherein the multilayer film (A) has beenstretched in the machine direction at a ratio in the range of from about5:1 to about 10:1.
 66. The labelstock of claim 56 wherein the adhesivelayer is a pressure-sensitive adhesive layer.
 67. The labelstock ofclaim 56 wherein the multilayer film (A) has been oriented in themachine direction at a stretch ratio of about 9:1 to about 10:1, andstretch oriented in the cross direction at a ratio of greater than 1:1up to about 3:1.
 68. The labelstock of claim 67 wherein the stretchratio in the cross direction is less than 2:1.
 69. A pressure-sensitiveadhesive label die-cut from the labelstock of claim
 56. 70. Adie-cuttable, biaxially stretch oriented monolayer film comprising atleast one polyolefin wherein the film has been stretch oriented in themachine direction at a stretch ratio of about 9:1 to about 10:1, and inthe cross direction at a stretch ratio of from greater than 1:1 to about3:1.
 71. The film of claim 70 wherein the stretch ratio in the crossdirection is less than 2:1.
 72. The film of claim 70 wherein the filmcomprises, polyethylene, a propylene polymer or copolymer, or mixturesthereof.
 73. The film of claim 70 wherein the film comprises a copolymeror propylene and ethylene or at least one α-olefin containing from 4 toabout 8 carbon atoms.
 74. A die-cuttable, stretch oriented multilayerfilm comprising (A) a base layer having an upper surface and a lowersurface, and comprising at least one polyolefin, (B) a first skin layerof thermoplastic polymers bonded to the upper surface of the base layerwherein the multilayer film has been stretch oriented in the machinedirection at a stretch ratio of from 9:1 to about 10:1, and in the crossdirection at a stretch ratio of greater than 1:1 to about 3:1.
 75. Themultilayer film of claim 71 wherein the multilayer film has been stretchoriented in the cross direction at a ratio of less than 2:1.